Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
1
vote
1
reply
1.1k
views
Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: gender determination and chrX CN calls
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: gender determination and chrX CN calls
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: gender determination and chrX CN calls
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
1
vote
0
replies
1.9k
views
Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
1.9k
views
Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
1.3k
views
Comment: Comment: Where do I get a WES dataset of size <1GB
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
1.3k
views
Comment: Comment: Where do I get a WES dataset of size <1GB
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
741
views
Comment: Comment: Genotyping variants from BAM (human)
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.4k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
3
votes
0
replies
759
views
Comment: Comment: Is reclustering of a cluster obtained from hierarchical clustering "allowed"?
2.7 years ago by German.M.Demidov ★ 2.9k
1
vote
0
replies
2.5k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
644
views
Comment: Comment: Should I run GISTIC2.0 for cases/controls separately?
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
1.2k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
1.2k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
1.2k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
2.7 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.5k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.7 years ago by German.M.Demidov ★ 2.9k
1
vote
1
reply
1.8k
views
Comment: Comment: Collect COV file by BedCoverage
2.8 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
704
views
Comment: Comment: Linear versus affine gap cost
2.8 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
1.2k
views
Comment: Comment: CNVkit Feedback about panel or normales needed
2.8 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
872
views
Comment: Comment: What is the well-recognized standard of coverage uniformity
2.8 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
1.2k
views
Comment: Comment: CNVkit Feedback about panel or normales needed
2.8 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
1.4k
views
Comment: Comment: UMAP and "equal" objects
2.9 years ago by German.M.Demidov ★ 2.9k
1
vote
0
replies
534
views
Comment: Comment: Control-FREEC significance
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
711
views
Comment: Comment: X-transposed region on chromosome Y
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
635
views
Comment: Comment: Ideas to represent RNA-seq expression profile (Z-scores) and the significance le
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
664
views
Comment: Comment: copy number variation and aneuploidy
2.9 years ago by German.M.Demidov ★ 2.9k
1
vote
1
reply
1.5k
views
Comment: Comment: what does very low estimates but a significant P value mean.
2.9 years ago by German.M.Demidov ★ 2.9k
1
vote
0
replies
1.5k
views
Comment: Comment: what does very low estimates but a significant P value mean.
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
841
views
Comment: Comment: Is WGS reliable for larges indels and duplication?
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
577
views
Comment: Comment: What can you detect with PE150bp shotgun sequencing with 100X depth
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
1.1k
views
Comment: Comment: Count the numfer of reads supporting a pattern from a BAM file
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
969
views
Comment: Comment: Check all pathogenics variants
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
841
views
Comment: Comment: Is WGS reliable for larges indels and duplication?
2.9 years ago by German.M.Demidov ★ 2.9k
1
vote
0
replies
630
views
Comment: Comment: Can we detect anapleuoids with sequencing (WGS 30X)?
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.6k
views
Comment: Comment: Regression assumptions - fitted and residual plots
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
1.3k
views
Comment: Comment: KING relatedness inference working way too long...
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
947
views
Comment: Comment: how to properly run TrioCNV for trios CNV detection
2.9 years ago by German.M.Demidov ★ 2.9k
1
vote
1
reply
947
views
Comment: Comment: how to properly run TrioCNV for trios CNV detection
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
0
replies
2.2k
views
Comment: Comment: [CONCEPTUAL] Mutant analysis - should the t-test be paired or unpaired?
2.9 years ago by German.M.Demidov ★ 2.9k
0
votes
1
reply
2.2k
views
Comment: Comment: [CONCEPTUAL] Mutant analysis - should the t-test be paired or unpaired?
2.9 years ago by German.M.Demidov ★ 2.9k
565 results • Page 3 of 12
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6